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Results: 21 to 30 of 30

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cataract

Asper Biogene Asper Biogene LLC
Estonia
4544
  • C Sequence analysis of the entire coding region

Cataract Panel

Blueprint Genetics
Finland
169
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Diseases - panels

MGZ Medical Genetics Center
Germany
6167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing SLC16A12

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Cataract Panel

CeGaT GmbH
Germany
2441
  • C Sequence analysis of the entire coding region

Cataract

MGZ Medical Genetics Center
Germany
265
  • C Sequence analysis of the entire coding region

SLC16A12 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Solute carrier family 16, member 12 deficiency (SLC16A12)

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 30 of 30

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.